Selection procedure reference: EMA/TR/11362
Deadline for applications: 06 May 2026 23:59 CET
The European Medicines Agency (EMA) is a decentralised agency of the European Union (EU), located in Amsterdam. It began operating in 1995. It is responsible for the scientific evaluation, supervision and safety monitoring of medicines in the EU.
This traineeship opportunity is now open for applications until 06 May 2026 23:59 CET, with an intake on 1 October 2026.
About the traineeship programme
The Agency is looking for motivated, qualified recent graduates or students on an Erasmus+ or other programme or PhD students or Master's students (who posses a previous degree), who are interested in gaining experience and contribute to the Agency’s work for every patient in Europe. The purpose of a traineeship at the Agency is to perform tasks that are predominantly in the interest of the trainee’s training and principally serve to increase the trainee’s knowledge and to gain relevant experience.
Placement description
We are looking for a trainee in the Labeling Office.
Specific objectives and projects
The project entails:
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mapping of existing labelling-related regulatory guidance and internal data, and translating it into a digitally structured, intuitive and user-friendly resource to support applicants in the preparation of invented names requests, product information annexes and associated mock-ups.
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analysing the mobile scanning technologies and other digital solutions in the labelling and package leaflet currently approved for centrally authorised medicinal products.
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exploring the potential application of existing and emerging cross-agency tools to determine how they can be used to enhance existing guidance, improve its accessibility for users, and support the optimisation of regulatory workflows and processes.
Learning outcomes
Through this project, the trainee will:
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Increase knowledge of EMA activities and the EU regulatory network.
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Acquire in-depth regulatory knowledge and experience in the area of medicinal products labelling.
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Acquire hands-on experience with the use of novel technologies and digital means in core regulatory processes.
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Be at the forefront of streamlining regulatory processes.
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Build experience working with a diverse and cross-functional team
Eligibility criteria
To be eligible for consideration for this placement, you are required to:
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enjoy full rights as a citizen of a European Union Member State or Iceland, Lichtenstein and Norway;
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possess a university degree in Pharmacy or Life Sciences (minimum of three years or more) that must have been obtained between 6 May 2025 and 6 May 2026 or be a university student on an Erasmus + or a similar programme or a PhD student or a Master's student with a previous fully finished degree in the areas mentioned before. A postgraduate qualification in Regulatory Affairs would be an advantage.
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a thorough knowledge of English (at least level C1) and good knowledge of other official EU language (at least B2) of the Common European Framework for Languages
For criteria 1 and 2, you will be required to provide proof in the application form and at the interview stage. Failing to present these documents may result in the disqualification from the procedure.
Additional skills
Excellent command of English, particularly in writing.
Strong analytical skills.
Proficiency in the use of digital tools.
Basic knowledge of EU pharmaceutical legislation.
Experience in project and process management would be desirable.
Behavioural Competencies
You will demonstrate the following behavioural competencies:
Conditions of traineeship
The traineeship is offered for 10 months (1 October 2026 – 31 July 2027) and takes place at the Agency’s premises in Amsterdam with possibility for teleworking up to 40% of working time from The Netherlands and occasional teleworking from outside The Netherlands. Traineeships are offered for either full-time or part-time (80% or 50%) if combined with university studies.
The Agency pays a monthly stipend of €2,049.77 for a full-time traineeship (reduced accordingly for 80% or 50%) and a travel contribution upon joining the Agency.
Each trainee will have a mentor at the Agency who will guide the trainee through the programme.
The conditions of employment are stated in the Executive Decision on rules governing the traineeship programme at the EMA available here .
Expected selection timelines
Deadline for applications
06 May 2026 23:59 CET
Assessments (remote)
From mid-June 2026 to mid-July 2026
Decision and offers
By end of July 2026
Placement start
1 October 2026
Domenico Scarlattilaan 6 - 1083 HS Amsterdam - The Netherlands
Telephone +31 (0)88 781 6000 - Email recruitment@ema.europa.eu
© European Medicines Agency, 2024. Reproduction is authorised provided the source is acknowledged.